Is a genetic defect in Fkbp6 a common cause of azoospermia in humans?

FK506-binding protein 6 (Fkbp6) is a member of a gene family containing a prolyl isomerase/FK506-binding domain and tetratricopeptide protein-protein interaction domains. Recently, the targeted inactivation of Fkbp6 in mice has been observed to result in aspermic males and the absence of normal pach...

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Detalles Bibliográficos
Autores principales: Miyamato, Toshinobu, Sato, Hisashi, Yogev, Leah, Kleiman, Sandra, Namiki, Mikio, Koh, Eitetsu, Sakugawa, Naoko, Hayashi, Hiroaki, Ishikawa, Mutsuo, Lamb, Dolores J., Sengoku, Kazuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Versita 2006
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6275806/
https://www.ncbi.nlm.nih.gov/pubmed/16983454
http://dx.doi.org/10.2478/s11658-006-0043-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6275806/
https://www.ncbi.nlm.nih.gov/pubmed/16983454
http://dx.doi.org/10.2478/s11658-006-0043-1

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